反应 #50686

ord-489d0133ade44cc9bcb67c29672dfe80

反应方程式

Nn1ccc(C(=O)c2ccccc2)c1
(1-amino-1H-pyrrol-3-yl)phenylmethanone
O=C(O)CNC(=O)OCc1ccccc1
N-carbobenzyloxyglycine
C(=NC1CCCCC1)=NC1CCCCC1
DCC
O=C(CNC(=O)OCc1ccccc1)Nn1ccc(C(=O)c2ccccc2)c1
Phenylmethyl-[2-[(3-benzoyl-1H-pyrrol-1-yl)amino]-2-oxoethyl]carbamate

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤filtered
  2. 2
    洗涤The filter cake was washed with ethyl acetate
  3. 3
    其他the combined filtrates were evaporated in vacuo
  4. 4
    其他The residual oil was purified by preparative HPLC (silica gel, DCM/ethyl acetate 3:1)
  5. 5
    其他Evaporation of the desired fractions
  6. 6
    其他afforded a colorless oil, which
  7. 7
    其他was crystallized from DCM/ethyl ether yielding the product as colorless crystals (5.96 g), m.p. 144°-145° C.

实验过程

To a solution of (1-amino-1H-pyrrol-3-yl)phenylmethanone (5.96 g) and N-carbobenzyloxyglycine (6.69 g) in 70 ml of anhydrous DCM and 30 ml of anhydrous dimethylformamide was added DCC (7.22 g). The reaction mixture was stirred at room temperature for 4 hours and filtered. The filter cake was washed with ethyl acetate, and the combined filtrates were evaporated in vacuo. The residual oil was purified by preparative HPLC (silica gel, DCM/ethyl acetate 3:1). Evaporation of the desired fractions afforded a colorless oil, which was crystallized from DCM/ethyl ether yielding the product as colorless crystals (5.96 g), m.p. 144°-145° C.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05428053uspto-grants-1995_06